ENST00000377833.10:c.7190T>G
MANE Select
|
ENSP00000367064.4:p.Ile2397Ser
|
|
ENST00000377833.8:c.7190T>G
|
ENSP00000367064.4:p.Ile2397Ser
|
|
NM_001081.3:c.7190T>G , LRG_540t1:c.7190T>G
|
NP_001072.2:p.Ile2397Ser
|
|
XM_011519708.1:c.7190T>G
|
XP_011518010.1:p.Ile2397Ser
|
|
XM_011519709.1:c.3176T>G
|
XP_011518011.1:p.Ile1059Ser
|
|
XM_011519710.1:c.3152T>G
|
XP_011518012.1:p.Ile1051Ser
|
|
XM_011519711.1:c.3032T>G
|
XP_011518013.1:p.Ile1011Ser
|
|
XM_011519708.2:c.7190T>G
|
XP_011518010.1:p.Ile2397Ser
|
|
XM_011519709.2:c.3176T>G
|
XP_011518011.1:p.Ile1059Ser
|
|
XM_011519710.2:c.3152T>G
|
XP_011518012.1:p.Ile1051Ser
|
|
XM_011519711.3:c.3032T>G
|
XP_011518013.1:p.Ile1011Ser
|
|
NM_001081.4:c.7190T>G
MANE Select
|
NP_001072.2:p.Ile2397Ser
|
|